Remote Clinical Trials Coordinator & SME – Drive Study Success

Merck; Juneau (AK); Remote; USD 74,000 - 118,000; Full time

Benefits offered by this job

Annual bonus

Long-term incentive

Medical, dental, vision

401(k) retirement

Paid holidays & vacation

Sick days

Job summary

Merck & Co., Inc. is seeking a Clinical Trial Coordinator to handle trial and site administration, document management, and regulatory support. You will collaborate with cross-functional teams to maintain CTMS trackers and ensure timely submissions.

The role requires at least 3 years in clinical research, a bachelor’s degree, and strong Excel/Office skills. It offers remote work options, up to 10% travel, and a comprehensive benefits package with annual bonus and long-term incentives.

Qualifications

• Minimum 3 years in Clinical Research or relevant healthcare experience.
• Completed job training (office management, administration, finance, health care preferred) or Bachelor’s Degree.

Responsibilities

• Trial and site administration: track essential documents, report safety results, manage study tools and documents, update CTMS and trackers, coordinate clinical/non-clinical supply.
• Document management: prepare and distribute documents, archive eTMF, assist with reconciliation and quality control.
• Regulatory & Site Start-Up: gather forms for start-up, obtain/update study insurance, support IRB/ERC submissions and regulatory packages.
• Budgeting, Agreement and Payments: develop and maintain country/site budgets and CTRAs, track contracts and payments, ensure compliance.

Skills

Clinical Research

CTA

GCDMP

Time Management

Training Delivery

Microsoft Excel

Microsoft Office

Leadership

Communication

Education

Bachelor’s Degree

Tools

CTMS

MS Excel

Job description

Merck & Co., Inc. is seeking a Clinical Trial Coordinator to handle trial and site administration, document management, and regulatory support. You will collaborate with cross-functional teams to maintain CTMS trackers and ensure timely submissions.

The role requires at least 3 years in clinical research, a bachelor’s degree, and strong Excel/Office skills. It offers remote work options, up to 10% travel, and a comprehensive benefits package with annual bonus and long-term incentives.